THE EQUALIZER AIRWAY DEVICE— 510(k) K870501

Name: FDA 510(k) clearance K870501
Creator: U.S. Food and Drug Administration
Published: 1987-03-04

Substantially Equivalent

Sleep Renewal, Inc.

FDA 510(k) clearance K870501 for THE EQUALIZER AIRWAY DEVICE, Substantially Equivalent on 1987-03-04. Applicant: Sleep Renewal, Inc.. Device class: 2.

Clearance details

Applicant: Sleep Renewal, Inc.
Product code: Code LQZ
Device class: Class 2
Regulation: 21 CFR 872.5570
Advisory panel: Dental
Date received: 1987-02-04
Decision date: 1987-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mobile, AL, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.